Detalhe da pesquisa
1.
Variants in CLDN5 cause a syndrome characterized by seizures, microcephaly and brain calcifications.
Brain
; 146(6): 2285-2297, 2023 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36477332
2.
Heterozygous loss of function of NR4A2 is associated with intellectual deficiency, rolandic epilepsy, and language impairment.
Clin Case Rep
; 7(8): 1582-1584, 2019 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-31428396